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Pyrolysis of diterminally unsaturated, eight-member chains

Creator:: Fleming, Michael Paul
Resource Type:: Masters Thesis
Full Text:: : PYROLYSIS OF DITERMINALLY UNSATURATED, EIGHT-MEMBER CHAINS Abstract approved: Redacted for privacy Elliot

An investigation of the reaction of benzil with triphenylphosphorusmethylene

Creator:: Wiman, Robert Edgar
Resource Type:: Masters Thesis
Full Text:: scope ot the 'Wi tt.lg reac.tion (4) a a) OOllO + OHO b) + - + c) - + ?0% 5 d

Semihydrogenation in conjugated systems and its application in the synthesis of trienes

Creator:: Tashiro, John Toshiyuki
Resource Type:: Dissertation
Full Text:: (38) were able to hydrogenate the enyne compound B with Lindlar catalyst to give cis product in good

I. Isolation of certain toxic components of kraft mill waste and attempts to determine their structure. ; II. Studies of the mechanism of the cope rearrangement of 1,2-divinyl-1, 2-cyclohexanediol

Creator:: Banks, Richard Charles
Abstract:: PART I. A chemical examination of the materials toxic to fish in kraft pulp mill wastes has been made as part of a water pollution study. Thirty gallons of "foul condensate" from a typical kraft mill gave 14 g of organic material when extracted with methylene chloride, and an additional...
Resource Type:: Dissertation
Full Text:: - HEXANEDIOL Abstract approved: Elliot N. Marvell PART I. A chemical examination of the materials toxic to

Synthesis of some bicyclo[6.1.0] - nonane derivatives

Creator:: Wall, Robert Gene
Abstract:: Bicyclo [6.1.0] non-4-ene was prepared by two routes; (1) reaction of cis-cis-1, 5-cycloöctadiene with methylene iodide and zinc-copper couple, (2) sodium-methanol reduction of 9, 9-dibromobicyclo-[6.1.0] non-4-ene. The bicyclononene was characterized by its infrared spectrum, nuclear magnetic resonance spectrum and common physical properties. The olefin was hydrogenated to bicyclo [6.1.0] -...
Resource Type:: Masters Thesis
Full Text:: -ene (III) 23 A. From 1, 5- cyclobctadiene and methylene iodide 23 B. From 9, 9- dibromobicyclo C6

The rearrangement of 1, 1-dimethyl-2-oxo-1, 2-dihydronaphthalene

Creator:: Stephenson, John Louis
Resource Type:: Masters Thesis
Full Text:: , , Typ6A by Charlonc Ournell il b" \ ACKNOWLEOO mNT The author thanks Dr . Elliot N, Marvell

A study of the acid catalyzed rearrangement of 4-oxo-3, 3-dimethyl-3, 4-dihydrophenanthrene

Creator:: Imel, Arthur Madison
Resource Type:: Dissertation
Full Text:: ..clihJdropbeuautlU'eu. • .28 B•&T&ugeateut or 4-oso-•3 ,,..S.1rletbJ1...) 14.cllbydl-o. pbenauthl-eu

A study of the thermal stability of benzyl 2,4-dimethyl-6-propenylphenyl ether

Creator:: Dupzyk, Ronald Jene
Resource Type:: Masters Thesis
Full Text:: My Father ACKNOWLEDGMENT The author wishes to expreaa hia apprecia tion to Dr. Elliot N

The reaction of N-bromosuccinimide (I) with acetals

Creator:: Joncich, Micheal Joseph
Resource Type:: Masters Thesis
Full Text:: £rocedures 15 Iv. 1iiTL . Preparation of N-bronosuccirìixriide 17 B. Preptrt1on of Acetals 1

The mechanism of the para-Claisen rearrangement

Creator:: Teranishi, Roy, 1922-2000
Resource Type:: Dissertation
Full Text:: usefulness of the Claisen rearrangement in synthetic work, (b) its appli- cation as a tool in the study

ScholarsArchive@OSU

Pyrolysis of diterminally unsaturated, eight-member chains

An investigation of the reaction of benzil with triphenylphosphorusmethylene

Semihydrogenation in conjugated systems and its application in the synthesis of trienes

I. Isolation of certain toxic components of kraft mill waste and attempts to determine their structure. ; II. Studies of the mechanism of the cope rearrangement of 1,2-divinyl-1, 2-cyclohexanediol

Synthesis of some bicyclo[6.1.0] - nonane derivatives

The rearrangement of 1, 1-dimethyl-2-oxo-1, 2-dihydronaphthalene

A study of the acid catalyzed rearrangement of 4-oxo-3, 3-dimethyl-3, 4-dihydrophenanthrene

A study of the thermal stability of benzyl 2,4-dimethyl-6-propenylphenyl ether

The reaction of N-bromosuccinimide (I) with acetals

The mechanism of the para-Claisen rearrangement

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